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Spotlight on the relevance of mtDNA in cancer

Clinical & translational oncology, 2017-04, Vol.19 (4), p.409-418

2017

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SAT0005 A Meta-Analysis and A Functional Study with Transmitochondrial Cybrids Confirm The Role of The Mtdna Haplogroups in The Development of Incident Knee Osteoarthritis. Data from Check and Oai

Annals of the rheumatic diseases, 2016-06, Vol.75 (Suppl 2), p.665-665

2016

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In vitro studies help us to inderstand the relationship between mitochondrial DNA (MTDNA) haplogroups and OA pathogenesis

Osteoarthritis and cartilage, 2016-04, Vol.24, p.S143-S144

2016

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THU0017 In Vitro Studies Using Cybrids Show that Mtdna Haplogroup J and H have Different Mitochondrial Activity. A Possible Explanation to OA Pathogenesis

Annals of the rheumatic diseases, 2015-06, Vol.74 (Suppl 2), p.198-199

2015

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In vitro studies show that MTDNA haplogroup J and H are associated with different metabolic and inflammatory profile. A possible explanation to OA pathogenesis

Osteoarthritis and cartilage, 2015-04, Vol.23, p.A155-A155

2015

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Drosophila melanogaster mitochondrial DNA: gene organization and evolutionary considerations

Genetics (Austin), 1988-04, Vol.118 (4), p.649-663

Garesse, R

1988

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Mutation analysis in 16 patients with mtDNA depletion

Human mutation, 2003-04, Vol.21 (4), p.453-454

2003

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Animal mitochondrial biogenesis and function: a regulatory cross-talk between two genomes

Gene, 2001-01, Vol.263 (1-2), p.1-16

2001

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392 Genetic Basis of Heart Transplanted Hypertrophic Cardiomyopathy

The Journal of heart and lung transplantation, 2011, Vol.30 (4), p.S135-S135

2011

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Mitochondrial DNA remains intact during Drosophila aging, but the levels of mitochondrial transcripts are significantly reduced

The Journal of biological chemistry, 1993-09, Vol.268 (25), p.18891-18897

1993

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La reproducibilidad de las investigaciones biomédicas: Quo vadis?

Medicina clínica, 2016-05, Vol.146 (9), p.408-412

2016

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Differential Regulation of the Catalytic and Accessory Subunit Genes of Drosophila Mitochondrial DNA Polymerase

The Journal of biological chemistry, 2000-10, Vol.275 (42), p.33123-33133

2000

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Mitochondrial dysfunction associated with a mutation in the Notch3 gene in a CADASIL family

Neurology, 2001-10, Vol.57 (7), p.1235-1238

2001

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Increased muscle nucleoside levels associated with a novel frameshift mutation in the thymidine phosphorylase gene in a Spanish patient with MNGIE

Neuromuscular disorders : NMD, 2005-11, Vol.15 (11), p.775-778

2005

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Genomic organization and developmental pattern of expression of the engrailed gene from the brine shrimp Artemia

Development (Cambridge), 1993-08, Vol.118 (4), p.1209-1219

1993

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Drosophila Mitochondrial Transcription Factor B2 Regulates Mitochondrial DNA Copy Number and Transcription in Schneider Cells

The Journal of biological chemistry, 2004-06, Vol.279 (26), p.26900-26905

2004

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Human COA3 Is an Oligomeric Highly Flexible Protein in Solution

Biochemistry (Easton), 2016-11, Vol.55 (45), p.6209-6220

2016

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Drosophila Mitochondrial Transcription Factor B1 Modulates Mitochondrial Translation but Not Transcription or DNA Copy Number in Schneider Cells

The Journal of biological chemistry, 2005-04, Vol.280 (17), p.16815-16820

2005

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A Conserved Heptamer Motif for Ribosomal RNA Transcription Termination in Animal Mitochondria

Proceedings of the National Academy of Sciences - PNAS, 1994-06, Vol.91 (12), p.5368-5371

1994

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Mitochondrial haplogroups associated with end-stage heart failure and coronary allograft vasculopathy in heart transplant patients

European heart journal, 2012-02, Vol.33 (3), p.346-353

2012

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Myoglobinuria and COX deficiency in a patient taking cerivastatin and gemfibrozil

Neurology, 2003-01, Vol.60 (1), p.124-126

2003

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The β Subunit of the Drosophila melanogaster ATP Synthase: cDNA Cloning, Amino Acid Analysis and Identification of the Protein in Adult Flies

Biochemical and biophysical research communications, 1993-09, Vol.195 (2), p.785-791

1993

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A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with ocular myopathy

Neuromuscular disorders : NMD, 2001-07, Vol.11 (5), p.477-480

2001

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A Drosophila Model of Mitochondrial DNA Replication: Proteins, Genes and Regulation

IUBMB life, 2005-08, Vol.57 (8), p.555-561

2005

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Spotlight on the relevance of mtDNA in cancer

SAT0005 A Meta-Analysis and A Functional Study with Transmitochondrial Cybrids Confirm The Role of The Mtdna Haplogroups in The Development of Incident Knee Osteoarthritis. Data from Check and Oai

In vitro studies help us to inderstand the relationship between mitochondrial DNA (MTDNA) haplogroups and OA pathogenesis

THU0017 In Vitro Studies Using Cybrids Show that Mtdna Haplogroup J and H have Different Mitochondrial Activity. A Possible Explanation to OA Pathogenesis

In vitro studies show that MTDNA haplogroup J and H are associated with different metabolic and inflammatory profile. A possible explanation to OA pathogenesis

Drosophila melanogaster mitochondrial DNA: gene organization and evolutionary considerations

Mutation analysis in 16 patients with mtDNA depletion

Animal mitochondrial biogenesis and function: a regulatory cross-talk between two genomes

392 Genetic Basis of Heart Transplanted Hypertrophic Cardiomyopathy

OPA1 mutations induce mitochondrial DNA instability and optic atrophy ‘plus’ phenotypes

Mitochondrial DNA remains intact during Drosophila aging, but the levels of mitochondrial transcripts are significantly reduced

La reproducibilidad de las investigaciones biomédicas: Quo vadis?

Differential Regulation of the Catalytic and Accessory Subunit Genes of Drosophila Mitochondrial DNA Polymerase

Mitochondrial dysfunction associated with a mutation in the Notch3 gene in a CADASIL family

Increased muscle nucleoside levels associated with a novel frameshift mutation in the thymidine phosphorylase gene in a Spanish patient with MNGIE

Genomic organization and developmental pattern of expression of the engrailed gene from the brine shrimp Artemia

Drosophila Mitochondrial Transcription Factor B2 Regulates Mitochondrial DNA Copy Number and Transcription in Schneider Cells

Human COA3 Is an Oligomeric Highly Flexible Protein in Solution

Drosophila Mitochondrial Transcription Factor B1 Modulates Mitochondrial Translation but Not Transcription or DNA Copy Number in Schneider Cells

A Conserved Heptamer Motif for Ribosomal RNA Transcription Termination in Animal Mitochondria

Mitochondrial haplogroups associated with end-stage heart failure and coronary allograft vasculopathy in heart transplant patients

Myoglobinuria and COX deficiency in a patient taking cerivastatin and gemfibrozil

The β Subunit of the Drosophila melanogaster ATP Synthase: cDNA Cloning, Amino Acid Analysis and Identification of the Protein in Adult Flies

A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with ocular myopathy

A Drosophila Model of Mitochondrial DNA Replication: Proteins, Genes and Regulation

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